Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

9.1%

1 terminated/withdrawn out of 11 trials

Success Rate

75.0%

-11.6% vs industry average

Late-Stage Pipeline

45%

5 trials in Phase 3/4

Results Transparency

33%

1 of 3 completed trials have results

Key Signals

3 recruiting1 with results

Enrollment Performance

Analytics

Phase 3
4(40.0%)
Phase 2
2(20.0%)
Phase 1
2(20.0%)
N/A
1(10.0%)
Phase 4
1(10.0%)
10Total
Phase 3(4)
Phase 2(2)
Phase 1(2)
N/A(1)
+1 more

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (11)

Showing 11 of 11 trials
NCT07759804Phase 4Not Yet Recruiting

A Study of Inhaled Treprostinil (LIQ861) in Adults With Pulmonary Arterial Hypertension Transitioning From Oral Selexipag

Role: lead

NCT07748000Phase 2Not Yet Recruiting

A Study of LIQ861 (Inhaled Treprostinil) in Adults With Systemic Sclerosis Who Have Symptomatic Raynaud's Phenomenon Attacks

Role: lead

NCT07561034Not ApplicableRecruiting

The Benefits of Home Exercise in Pulmonary Hypertension Interstitial Lung Disease

Role: collaborator

NCT07285655Phase 3Recruiting

A Phase 3 Study to Evaluate the Safety and Efficacy L606 in Participants With PH-ILD

Role: lead

NCT06129240Recruiting

An Open-Label ProSpective MultiCENTer Study to Evaluate Safety and Tolerability of Dry Powder Inhaled Treprostinil in PH

Role: lead

NCT04691154Phase 3Active Not Recruiting

A Phase 3 Study to Evaluate the Safety and Tolerability of L606 in Subjects With PAH or PH-ILD

Role: lead

NCT03992755Phase 3Active Not Recruiting

Extension Study for Participants in LIQ861 Trials to Evaluate the Long-term Safety of Dry Powder Inhalation of Treprostinil

Role: lead

NCT03399604Phase 3Completed

Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil

Role: lead

NCT03884465Phase 2Terminated

Hemodynamic Evaluation of Dose-response and Safety of Dry Powder Inhalation of Treprostinil

Role: lead

NCT02982889Phase 1Completed

Single Ascending Dose Study of Two Liquidia Bupivacaine Formulations

Role: lead

NCT01224262Phase 1Completed

A Study Evaluating the Safety and Tolerability of a Seasonal Influenza Vaccine Containing LIQ001

Role: lead

All 11 trials loaded